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88,000+ live jobsSenior TMF Associate
On-site in Barcelona·Added 5 days ago (last checked 27 Oct)
9 open roles
Our summary
- Work mode
- On-site, Barcelona
- English
- Required
- Experience
- 6+ years
- Education
- University degree




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Skills
Requirements
Education & certifications
• University degree in Life Sciences, Information Management, Library or Archival Science, or a relevant discipline.
• Fluent professional English
• Minimum 6+ years of relevant TMF, clinical documentation or clinical operations experience, including substantial direct TMF responsibility.
• Demonstrated autonomous sponsor-side or equivalent oversight across multiple studies and CRO delivery models.
• Experience with TMF quality metrics, issue management, transfers, reconciliation, verification and archiving.
• Working knowledge of Veeva Vault eTMF or eTMF Archive and of ICH-GCP, GxP and ALCOA+ principles.
• Ability to work independently, manage competing priorities and deliver clear, traceable outputs.
Pay & benefits
What you'll get
We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality, and making a difference in the lives of patients.
Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation, and a shared commitment to excellence. Together, we make a difference.
The role
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.
The Senior TMF Associate provides autonomous sponsor-side oversight of TMF activities across assigned clinical studies and supports compliant management of the R&D archive. The role works with CROs, study teams, Quality and Information Technology to maintain TMF quality, inspection readiness, reliable transfer and archiving, and clear traceability of risks, decisions and actions.
As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area.
What you'll do
• Provide sponsor-side TMF oversight from study set-up through close-out, transfer and archiving.
• Review TMF Plans, TMF Indexes, Expected Document Lists and CRO oversight arrangements.
• Monitor TMF completeness, quality and timeliness; identify gaps and coordinate corrective follow-up.
• Guide study teams and CROs on TMF responsibilities, document expectations and inspection readiness.
• Coordinate TMF transfers, mapping, reconciliation and risk-based post-transfer verification.
• Support Veeva Vault eTMF Archive activities, including study set-up, access, UAT and operational support.
• Maintain portfolio tracking of TMF locations, transfers, archived records, findings and ownership.
• Draft and improve TMF SOPs, Work Instructions, templates, checklists, guidance and training materials.
• Maintain the R&D archive and coordinate custody, retrieval, shipments, records controls and archive vendors.
• Support audits and inspections and provide concise status updates on risks, overdue actions and decisions.
About TFS HealthScience
TFS HealthScience is a global contract research organization (CRO) that partners with pharmaceutical, biotechnology, and medical device companies to bring new treatments to market. With over 30 years of experience, the company provides a comprehensive range of clinical development services, including project management, clinical monitoring, data management, biostatistics, regulatory affairs, and quality assurance. TFS operates across North America, Europe, and Asia, employing a team of clinical and scientific professionals dedicated to advancing healthcare through efficient and compliant clinical trials.
In Spain, TFS HealthScience has established a strong presence with offices in Madrid and Barcelona, serving as a key hub for clinical operations in Southern Europe. The company is known for its collaborative and supportive work culture, offering international professionals the opportunity to work on diverse therapeutic areas and global studies. For those relocating to Spain, TFS provides a dynamic environment that values professional growth, cross-cultural collaboration, and work-life balance, making it an attractive employer for clinical research and quality management experts.
- Founded
- 1991
- Employees
- 500–1,000
- Headquarters
- Montreal, Canada
- In Spain
- Madrid, Barcelona
Good to know if you are moving
- TFS HealthScience has offices in Madrid and Barcelona, offering international professionals a chance to work in two of Spain's most vibrant cities.
- The company is a global CRO, meaning employees often collaborate on international clinical trials, providing exposure to diverse therapeutic areas and global regulatory standards.
- TFS offers roles in clinical operations, quality management, and business development, which are in high demand in Spain's growing life sciences sector.
- The company's work culture emphasizes professional development and work-life balance, which is well-aligned with the Spanish lifestyle.
- As a mid-sized CRO, TFS may offer more opportunities for cross-functional collaboration and faster career progression compared to larger organizations.
In their own words
About the company & team
Our journey began over 30 years ago in Sweden, in the city of Lund. As a full-service global CRO, we build solution-driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.
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